NM_000393.5(COL5A2):c.1977+6T>A AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 23, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000196369.2
Allele description [Variation Report for NM_000393.5(COL5A2):c.1977+6T>A]
NM_000393.5(COL5A2):c.1977+6T>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022